Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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  - Gene tree
  - Orthologues
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Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
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External references
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ID History
- Gene history

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Gene: LRIF1 ENSSSCG00000006799

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Description

ligand dependent nuclear receptor interacting factor 1 [Source:VGNC Symbol;Acc:VGNC:89809]

Location

Primary_assembly 4: 109,271,728-109,292,310 forward strand.

Sscrofa11.1:CM000815.5

About this gene

This gene has 1 transcript (splice variant) and 171 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000007447.4	LRIF1-201	4897	762aa	ENSSSCP00000007252.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1TAV2 F1S629	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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